Clinical Research Coordinator in São Paulo, Brazil (Fixed term & Part time)

BZL IQVIA RDS Brasil Ltda; São Paulo; Presencial; BRL 80.000 - 120.000; Tempo parcial

Resumo da oferta

A leading global clinical research company in São Paulo is seeking a Clinical Research Coordinator to work part-time for 24 hours a week on a 6-month contract. Responsibilities include verifying research study information, data input into EDC systems, and assisting with regulatory documents. The ideal candidate will have a bachelor's in life sciences and experience in clinical trials. This role offers flexibility and supports career progression.

Qualificações

• Experience in clinical research or nursing background.
• Availability to work part-time (24 hours per week).
• Availability to work in a fixed term contract (6 months).

Responsabilidades

• Verifying and correcting research study information on source documents.
• Accurate input of trial data into the Electronic Data Capture (EDC) system.
• Preparing and maintaining study files and timely submission of information.
• Collecting and maintaining relevant regulatory and ethics documents.
• Scheduling visits with research subjects and generating documentation.
• Other administrative support functions such as reception and office organization.

Conhecimentos

Basic knowledge of clinical trials

Study coordinator experience

Formação académica

Bachelor's degree in life sciences

Descrição da oferta de emprego

Overview

Are you looking for an opportunity in Clinical Research? You want to work for an industry leading company that offers experience and supports career progression whilst giving you the option of working flexibly? If so, come and join us - IQVIA are looking for a Clinical Research Coordinator.

This role has an immediate start working 24 hours a week for a period of 6 months to support the site. The study coordinator should have experience clinically or nursing background as tasks include performing EKG, collecting vital signs.

This is an excellent opportunity if you have experience working as a SC

As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.

Day to day responsibilities

• Verifying and/or correcting research study information on source documents; researching queries and variances; providing feedback to the site data collector
• Accurate input of trial data into the Electronic Data Capture (EDC) system and tracking visits and procedures completed against budget in the clinical trial management system (CTMS)
• Preparing and maintaining study files, and timely submission of information
• Collecting, submitting and assisting in maintaining relevant regulatory and ethics documents
• Scheduling visits with research subjects, generating appropriate reports and documentation
• Other administrative support functions such as reception, office organization and supply management

Qualifications and experience

• Bachelor's degree in life sciences
• Basic knowledge of clinical trials, study coordinator experience
• Availability to work based in São Paulo
• Availability to work part-time (24 hours per week)
• Availability to work in a fixed term contract (6 months)

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com